chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 47459082 47459085 GTG 54 GENIC homozygous 144438752 13 47460870 47460871 T G 47 GENIC homozygous 139289170 13 47460353 47460354 T A 62 GENIC homozygous 139289167 13 47460289 47460290 C T 61 GENIC homozygous 139289166 13 47460392 47460393 G A 67 GENIC homozygous 139289168 13 47460521 47460522 T A 52 GENIC homozygous 139289169 13 47460934 47460935 G A 48 GENIC homozygous 139289171 13 47461071 47461072 C T 54 GENIC possibly homozygous 139289172 13 47461188 47461189 T C 60 GENIC homozygous 139289173 13 47461194 47461195 A G 61 GENIC homozygous 139289174 13 47462582 47462583 G A 67 GENIC homozygous 139289175 13 47463800 47463801 T C 55 GENIC homozygous 139289177 13 47466485 47466486 T 39 GENIC possibly homozygous 139171931 13 47466991 47466992 T C 59 GENIC homozygous 139289186 13 47467345 47467346 A G 63 GENIC homozygous 139289188 13 47471837 47471838 A G 56 GENIC homozygous 139289190 13 47472400 47472404 GTGG 37 GENIC homozygous 139171937 13 47474284 47474291 CGTGCGT 20 GENIC homozygous 144438753 13 47473772 47473773 T G 62 GENIC homozygous 139289191 13 47467773 47467774 A G 56 GENIC homozygous 144444725 13 47468471 47468472 A G 59 GENIC homozygous 144444726 13 47470768 47470769 C G 60 GENIC homozygous 144444727 13 47473762 47473763 G A 61 GENIC homozygous 144444728 13 47474298 47474299 T 21 GENIC heterozygous 404022974 13 47474298 47474299 T G 21 GENIC homozygous 404022975 13 47474294 47474295 T 20 GENIC heterozygous 404022972 13 47474294 47474295 T G 20 GENIC homozygous 404022973 13 47474336 47474337 C T 37 GENIC homozygous 139289192 13 47475254 47475255 A G 57 GENIC homozygous 139289193